Canonical Allele Identifier: CA402465968

Gene: SMAD4

Linked Data

• dbSNP Id: rs2144478737
• MyVariant Identifiers: chr18:g.48604709C>G (hg19) ; chr18:g.51078339C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078339C>G , CM000680.2:g.51078339C>G	GRCh38
NC_000018.9:g.48604709C>G , CM000680.1:g.48604709C>G	GRCh37
NC_000018.8:g.46858707C>G	NCBI36
NG_013013.2:g.115300C>G , LRG_318:g.115300C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1531C>G	ENSP00000465878.2:p.Pro511Ala
ENST00000589076.6:c.1531C>G	ENSP00000466934.2:p.Pro511Ala
ENST00000589941.2:c.1531C>G	ENSP00000465874.2:p.Pro511Ala
ENST00000590061.2:c.1531C>G	ENSP00000464772.2:p.Pro511Ala
ENST00000593223.2:c.*1528C>G	ENSP00000466118.2:n.*1528C>G
ENST00000611848.2:c.*183C>G	ENSP00000478613.2:n.*183C>G
ENST00000684953.1:n.3546C>G
ENST00000685090.1:n.3461C>G
ENST00000685232.1:n.1752C>G
ENST00000688574.1:n.1639C>G
ENST00000691124.1:n.4492C>G
ENST00000342988.8:c.1531C>G MANE Select	ENSP00000341551.3:p.Pro511Ala
ENST00000342988.7:c.1531C>G	ENSP00000341551.3:p.Pro511Ala
ENST00000398417.6:c.1531C>G	ENSP00000381452.1:p.Pro511Ala
ENST00000586253.1:n.253C>G
ENST00000588745.5:c.1243C>G	ENSP00000464901.1:p.Pro415Ala
ENST00000591126.5:n.3532C>G
ENST00000592186.5:c.1178C>G	ENSP00000468611.1:n.1178C>G
ENST00000611848.1:c.844C>G
NM_005359.5:c.1531C>G , LRG_318t1:c.1531C>G	NP_005350.1:p.Pro511Ala
NM_005359.6:c.1531C>G MANE Select	NP_005350.1:p.Pro511Ala